Matthew S. Hestand

2.5k citations

26 papers · 1.2k indexed · 1 hit paper · h-index 16

Co-authors: Joris Vermeesch Adam Ameur Simon Ardui Wigard P. Kloosterman Koen Herten Johan T. den Dunnen Peter A.C. ’t Hoen Michiel van Galen
Topics: Genomics and Phylogenetic Studies (8 papers)Genomic variations and chromosomal abnormalities (7 papers)Congenital heart defects research (5 papers)
Cited by: Genetics Molecular Biology Cancer Research
Journals: Nucleic Acids Research PLoS ONE Genome Research
Partner nations: United States Belgium Netherlands

In The Last Decade

Matthew S. Hestand

26 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics

2018 493 citations Simon Ardui, Adam Ameur et al. Nucleic Acids Research profile →

Peers

Countries citing papers authored by Matthew S. Hestand

Since Specialization

Citations

This map shows the geographic impact of Matthew S. Hestand's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Matthew S. Hestand with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew S. Hestand more than expected).

Fields of papers citing papers by Matthew S. Hestand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew S. Hestand. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Matthew S. Hestand. The network helps show where Matthew S. Hestand may publish in the future.

Co-authorship network of co-authors of Matthew S. Hestand

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew S. Hestand. A scholar is included among the top collaborators of Matthew S. Hestand based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Matthew S. Hestand. Matthew S. Hestand is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Long‐read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalities 2024 ·American Journal of Medical Genetics Part A ·Kristen L. Sund,(unknown),Joyce Lee,John Garbe,Zakia Abdelhamed,(unknown),Barbara Hallinan,(unknown),(unknown),(unknown),Rolf W. Stottmann,Teresa A. Smolarek,Lisa Dyer,Matthew S. Hestand	3
2	Extreme enrichment of VNTR-associated polymorphicity in human subtelomeres: genes with most VNTRs are predominantly expressed in the brain 2020 ·Translational Psychiatry ·(unknown),(unknown),Matthew S. Hestand,Jonas Korlach,Joris Vermeesch,Marcel Reinders,Henne Holstege	17
3	Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition 2019 ·Genetics in Medicine ·Marta Unolt,Molka Kammoun,Beata Nowakowska,Gail E. Graham,T. Blaine Crowley,Matthew S. Hestand,(unknown),Maciej Geremek,Beverly S. Emanuel,Elaine H. Zackai,Joris Vermeesch,Donna M. McDonald‐McGinn	7
4	The 22q11 low copy repeats are characterized by unprecedented size and structural variability 2019 ·Genome Research ·(unknown),Yulia Mostovoy,Feyza Yilmaz,(unknown),Steven Pastor,Matthew S. Hestand,Ann Swillen,Elfi Vergaelen,Elizabeth A. Geiger,Curtis R. Coughlin,(unknown),Donna M. McDonald‐McGinn,Bernice E. Morrow,Pui–Yan Kwok,Ming Xiao,Beverly S. Emanuel,Tamim H. Shaikh,Joris Vermeesch	28
5	Single-Molecule Sequencing: Towards Clinical Applications 2018 ·Trends in biotechnology ·Adam Ameur,Wigard P. Kloosterman,Matthew S. Hestand	123
6	Conventional and Single-Molecule Targeted Sequencing Method for Specific Variant Detection in IKBKG while Bypassing the IKBKGP1 Pseudogene 2017 ·Journal of Molecular Diagnostics ·Glynis Frans,(unknown),Jutte van der Werff ten Bosch,Isabelle Meyts,Xavier Bossuyt,Joris Vermeesch,Matthew S. Hestand	22
7	Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing 2016 ·Human Mutation ·Simon Ardui,Valérie Race,(unknown),Matthew S. Hestand,Hilde Van Esch,Koenraad Devriendt,Gert Matthijs,Joris Vermeesch	31
8	A catalog of hemizygous variation in 127 22q11 deletion patients 2016 ·Human Genome Variation ·Matthew S. Hestand,Beata Nowakowska,Elfi Vergaelen,Jeroen Van Houdt,Luc Dehaspe,Joshua A. Suhl,Jurgen Del‐Favero,Geert Mortier,Elaine H. Zackai,Ann Swillen,Koenraad Devriendt,Raquel E. Gur,Donna M. McDonald‐McGinn,Stephen T. Warren,Beverly S. Emanuel,Joris Vermeesch	7
9	Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis 2016 ·Human Molecular Genetics ·Xingyi Guo,(unknown),(unknown),Raquel Castellanos,Matthew S. Hestand,Joris Vermeesch,Bernice E. Morrow,Deyou Zheng	14
10	Polymerase specific error rates and profiles identified by single molecule sequencing 2016 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Matthew S. Hestand,Jeroen Van Houdt,Francesca Cristofoli,Joris Vermeesch	40
11	A distinct class of chromoanagenesis events characterized by focal copy number gains 2016 ·(unknown),Matthew S. Hestand,Hilde Van Esch,Pascale Kleinfinger,(unknown),Alexandra Afenjar,(unknown),(unknown),(unknown),Joris Vermeesch	9
12	Tissue Restricted Splice Junctions Originate Not Only from Tissue-Specific Gene Loci, but Gene Loci with a Broad Pattern of Expression 2015 ·PLoS ONE ·Matthew S. Hestand,Zheng Zeng,S.J. Coleman,Jinze Liu,James N. MacLeod	4
13	Comparison of the Equine Reference Sequence with Its Sanger Source Data and New Illumina Reads 2015 ·PLoS ONE ·(unknown),Matthew S. Hestand,S.J. Coleman,Zheng Zeng,Ludovic Orlando,James N. MacLeod,Ted Kalbfleisch	7
14	Annotation of the Protein Coding Regions of the Equine Genome 2015 ·PLoS ONE ·Matthew S. Hestand,Ted Kalbfleisch,S.J. Coleman,Zheng Zeng,Jinze Liu,Ludovic Orlando,James N. MacLeod	23
15	Pseudoautosomal Region 1 Length Polymorphism in the Human Population 2014 ·PLoS Genetics ·Martin A. Mensah,Matthew S. Hestand,Maarten Larmuseau,Mala Isrie,Nancy Vanderheyden,(unknown),Erika Souche,Jeroen Van Houdt,Radka Stoeva,Hilde Van Esch,Koenraad Devriendt,Thierry Voet,Ronny Decorte,Peter N. Robinson,Joris Vermeesch	21
16	Analysis of Unannotated Equine Transcripts Identified by mRNA Sequencing 2013 ·PLoS ONE ·S.J. Coleman,Zheng Zeng,Matthew S. Hestand,Jinze Liu,James N. MacLeod	15
17	Tissue-specific transcript annotation and expression profiling with complementary next-generation sequencing technologies 2010 ·Nucleic Acids Research ·Matthew S. Hestand,Andreas Klingenhoff,Matthias Scherf,Yavuz Ariyürek,Y.F. Ramos,Wilbert van Workum,Makoto Suzuki,Thomas Werner,Gert‐Jan B. van Ommen,Johan T. den Dunnen,Matthias Harbers,Peter A.C. ’t Hoen	27
18	Genome-wide assessment of differential roles for p300 and CBP in transcription regulation 2010 ·Nucleic Acids Research ·Y.F. Ramos,Matthew S. Hestand,(unknown),(unknown),Yavuz Ariyürek,Michiel van Galen,Hans van Dam,G.J.B. van Ommen,Johan T. den Dunnen,A. Zantema,Peter A.C. ’t Hoen	114
19	CORE_TF: a user-friendly interface to identify evolutionary conserved transcription factor binding sites in sets of co-regulated genes 2008 ·BMC Bioinformatics ·Matthew S. Hestand,Michiel van Galen,(unknown),Gert‐Jan B. van Ommen,Johan T. den Dunnen,Peter A.C. ’t Hoen	32
20	CanineCOL4A3andCOL4A4: Sequencing, mapping and genomic organization 2005 ·DNA sequence ·(unknown),L. V. Millon,Matthew S. Hestand,Bernard A. van Oost,Danika L. Bannasch	3

About Matthew S. Hestand

Matthew S. Hestand is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 26 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Genetics (346 citations), Molecular Biology (812 citations) and Cancer Research (153 citations). Matthew S. Hestand has collaborated with scholars based in United States, Belgium and Netherlands. Frequent co-authors include Joris Vermeesch, Adam Ameur, Simon Ardui, Wigard P. Kloosterman, Koen Herten, Johan T. den Dunnen, Peter A.C. ’t Hoen, Michiel van Galen, Y.F. Ramos and Yavuz Ariyürek. Their work appears in journals such as Nucleic Acids Research, PLoS ONE and Genome Research.

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